chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55655520956555210CA13GENIChomozygous113811620
55655563956555640GC42GENIChomozygous113811622
55655610056556101TG36GENIChomozygous113811624
55655687156556872AC34GENIChomozygous113811626
55655739456557395TC53GENIChomozygous113811628
55655883856558839AT29GENIChomozygous113811630
55655903656559037AG20GENIChomozygous113811632
55655949856559499AT27GENIChomozygous113811634
55655986656559867TC31GENIChomozygous113811636
55656006956560070GA34GENICheterozygous113811638
55656016356560164CT33GENICheterozygous113811640
55656024056560241AT27GENICheterozygous114501407
55656075656560757CT49GENICheterozygous114117360
55656078356560784AG22GENICpossibly homozygous113811642
55656080256560803CT29GENICheterozygous113811646
55656081356560814AG29GENICheterozygous114117362
55656093156560932CT38GENIChomozygous113811648
55656100456561005AG27GENIChomozygous113811650
55656114056561141GT16GENIChomozygous113811652
55656189356561894AT45GENICheterozygous114501409
55656190156561902AT43GENICheterozygous114330383
55656208056562081CT26GENIChomozygous113811654
55656254656562547TC18GENIChomozygous113811656
55656318756563188TC29GENIChomozygous113811658
55656330756563308TA33GENIChomozygous113811660
55656435356564354CA31GENIChomozygous113811662
55656514356565144TG23GENIChomozygous113811664
55656521156565212AG31GENIChomozygous113811666
55656583756565838CT21GENIChomozygous113811668
55656616956566170TC29GENIChomozygous113811670
55656621356566214GA31GENIChomozygous113811672